A new computational algorithm is introduced for solving scattering problem in periodic structure. The PML technique is used to deal with the difficulty on truncating the unbounded domain while the DSC algorithm is uti...A new computational algorithm is introduced for solving scattering problem in periodic structure. The PML technique is used to deal with the difficulty on truncating the unbounded domain while the DSC algorithm is utilized for the spatial discretization. The present study reveals that the method is efficient for solving the problem.展开更多
Layered compounds play pivotal roles as precursors for producing 2D materials through mechanical exfoliation(micro-mechanical cleavage) or chemical approaches. Therefore, searching for layered compounds with sharp ani...Layered compounds play pivotal roles as precursors for producing 2D materials through mechanical exfoliation(micro-mechanical cleavage) or chemical approaches. Therefore, searching for layered compounds with sharp anisotropic chemical bonding and properties becomes emergent. In this work, the stability, electronic structure, elastic properties, and lattice dynamics of YBCwere investigated. Strong anisotropy in elastic properties is revealed, i.e., high Young’s modulus in a-b plane but low Young’s modulus in c direction. The maximum to minimum Young’s modulus ratio is 2.41 and 2.45 for YBCwith P42/mmc and P4/mbm symmetry, respectively. The most likely systems for shear sliding or microdelaminating are(001)[100] and(001)[010]. The anisotropic elastic properties are underpinned by the anisotropic chemical bonding, i.e., strong bonding within the BCnets and weak bonding between Y atom layers and BCnets. YBCis electrically conductive and the contributions to the electrical conductivity are from delocalized Y 4deas well as Bpandpzelectrons. The layered crystal structure, sharp anisotropic mechanical properties, and metallic conductivity endorse YBCpromising as a precursor for new 2D BCnets.展开更多
The samples of the C-S-H series were synthesized by hydrothermal reaction of fumed silica, CaO and deionized water at initial C/S ratios between 1.0-1.7. Phase composition and structural and morphology characteristics...The samples of the C-S-H series were synthesized by hydrothermal reaction of fumed silica, CaO and deionized water at initial C/S ratios between 1.0-1.7. Phase composition and structural and morphology characteristics of C-S-H samples were analyzed by XRD, IR and SEM. The experimental results showed that the d-spacing of （002）, （110） and （020） decreased, the d-spacing of （200） increased, and the d-spacing of （310） varied randomly, the polymerization of silica tetrahedra of C-S-H decreased, and morphology of C-S-H samples varied from sheet shapes to long reticular fibers as C/S ratio increased.展开更多
A key property of the boreal forest is that it stores huge amounts of carbon(C),especially belowground in the soil.Amounts of C stored in the uppermost organic layer of boreal forest soils vary greatly in space due to...A key property of the boreal forest is that it stores huge amounts of carbon(C),especially belowground in the soil.Amounts of C stored in the uppermost organic layer of boreal forest soils vary greatly in space due to an interplay between several variables facilitating or preventing C accumulation.In this study,we split C stocks into the organic layer and charcoal C due to their difference in origin,stability,and ecological properties.We compared organic layer C and charcoal C stocks in two regions of south-central Norway(Trillemarka and Varaldskogen),characterized by Scots pine and Norway spruce forests with varying fire histories.We used structural equation modeling to investigate how vegetation composition,hydrotopography,and soil properties interplay to shape organic layer C and charcoal C stocks.Pine forests consistently contained larger organic layer C stocks than spruce forests.Charcoal stocks,in contrast,were less consistent across both forest types and study regions as pine forests had higher charcoal C stocks than spruce forests in Trillemarka,while the two forest types contained equal charcoal C stocks in Varaldskogen.Charcoal and soil organic layer C stocks increased with higher fire frequencies(number of fire events over the last 600 years),but not with a shorter time since last fire(TSF).Additionally,vegetation composition,terrain slope,and soil moisture were the most important drivers of the organic layer C stocks,while charcoal C stocks were mainly controlled by the depth of the organic layer.Also,microtopography was of importance for organic layer C and charcoal C,since depressions in the forest floor had more charcoal C than well-drained minor hills.展开更多
According to specifications for Welding Procedure Qualification of ASME IX Section and Chinese code, JB 4708 2000, a software package for managing welding documents has been rebuilt. Consequently, the new software pa...According to specifications for Welding Procedure Qualification of ASME IX Section and Chinese code, JB 4708 2000, a software package for managing welding documents has been rebuilt. Consequently, the new software package can be used in a Limited Area Network (LAN) with 4 different levels of authorities for different users. Therefore, the welding documents, including DWPS (Design for Welding Procedure Specifications), PQRs (Procedure Qualification Records) and WPS (Welding Procedure Specifications) can be shared within a company. At the same time, the system provides users various functions such as browsing, copying, editing, searching and printing records, and helps users to make decision of whether a new PQR test is necessary or not according to the codes above as well. Furthermore, super users can also browse the history of record modification and retrieve the records when needed.展开更多
Based on S wave records of deep teleseisms on Digital Seismic Network of Shanxi Province, shear wave velocity structures beneath 6 stations were obtained by means of S wave waveform fitting. The result shows that the ...Based on S wave records of deep teleseisms on Digital Seismic Network of Shanxi Province, shear wave velocity structures beneath 6 stations were obtained by means of S wave waveform fitting. The result shows that the crust is thick in the studied region, reaching 40 km in thickness under 4 stations. The crust all alternatives high velocity layer with low velocity one. There appear varied velocity structures for different stations, and the stations around the same tectonic region exhibit similar structure characteristics. Combined with dominant depth distribution of many small-moderate earthquakes, the correlation between seismogenic layers and crustal structures of high and low velocity layers has been discussed.展开更多
Impurity formation energy, electronic structure, and photocatalytic properties of C-, N-, or S-doped BiOCl are investigated by density-functional theory plus U calculations(DFT + U). Results show that the doping effec...Impurity formation energy, electronic structure, and photocatalytic properties of C-, N-, or S-doped BiOCl are investigated by density-functional theory plus U calculations(DFT + U). Results show that the doping effect of S is better than that of C or N on the tunable photocatalytic activities of BiOCl. At low concentration, S-doped BiOCl systems are the most stable under Bi-rich growth conditions because of their lower impurity-formation energy. Compared with the electronic structures of S-doped BiOCl, C-or N-doped BiOCl have relatively deeper impurity energy levels appearing in their band gap(except Bi_(36)O_(35)NCl_(36)), which may act as photogenerated carrier-recombination centers and reduce photocatalytic activity. At high concentration, S is substituted on the O lattice site system, whereas some S 3p states mix with the valence band; this mixture leads to an obvious band-gap decrease and continuum-state formation above the valence-band edge of BiOCl. Such activity is advantageous to photochemical catalysis response. Compared with pure Bi OCl and a low-concentration S-doped system, a high-concentration S-doped system shows an obvious redshift on the absorption edge and has better photocatalytic O_2 evolution performance.展开更多
The effects of polyaerylamide （PAM） and polyvinyl alcohol （PVA） on morphology and structure of calcium silica~ hydrate with C/S 1.0-1.7 prepared via precipitation in solution were investigated by XRD, FT-IR and TE...The effects of polyaerylamide （PAM） and polyvinyl alcohol （PVA） on morphology and structure of calcium silica~ hydrate with C/S 1.0-1.7 prepared via precipitation in solution were investigated by XRD, FT-IR and TEM techniques. The results show that incorporation of the polymers decreased the order degree, increased the interlayer spacing and disturbed the layered stacking of C-S-H. Interlayer spacing expansion depended on C/S ratios and type of polymer. Interlayer spacing expansion had a minimum at C/S 1.0 and a maximum at C/S 1.3 and 1.5. Interlayer spacing expansion of PAM was bigger than that of PVA with the same C/S. C-S-H added with PVA mainly exhibited foil-like and fibrillar morphology. The fibrils were of variable length from a few tens of nanometers to a few hundreds of nanometers. Fibrils or foils seemed to be longer in the presence of PVA.展开更多
(PPh_3)_2Ni(i-mnt),(i-mnt=S_2C=C(CN)_2),Mr=613.43,monoclinic,Pn,a=9.167(3),b=10.872(3), c=18.209(7) ,β=101.46(3)°,V=1779(1) ,Z=2,Dc=1.15 g/cm^3,λ(Moka)=0.71069 ,μ=7.67 cm^(-1), F(000)=648,T=296K,final R=0.060,...(PPh_3)_2Ni(i-mnt),(i-mnt=S_2C=C(CN)_2),Mr=613.43,monoclinic,Pn,a=9.167(3),b=10.872(3), c=18.209(7) ,β=101.46(3)°,V=1779(1) ,Z=2,Dc=1.15 g/cm^3,λ(Moka)=0.71069 ,μ=7.67 cm^(-1), F(000)=648,T=296K,final R=0.060,Rw=0.073 for 1909 observed reflections with Ⅰ≥3σ(Ⅰ).The complex adopts a square planar geometry as its coordination unit,the mean Ni-S and Ni-P distances are 2.216 and 2.221 ,respectivety.展开更多
In the paper, dicalcium silicate (C2S) was modified to obtain higher performance, and the solutionizing pattern of BaSO4 in cement clinker was analyzed theoretically. According to experimental results, solutionizing o...In the paper, dicalcium silicate (C2S) was modified to obtain higher performance, and the solutionizing pattern of BaSO4 in cement clinker was analyzed theoretically. According to experimental results, solutionizing of BaSO4in cement clinker improved crystal plane distance of C2S as well as the relations of coordination. The performance tests show that the strength of C2S modified by BaSO4 changes and the reactivity of C2S increases significantly.展开更多
(CH_3C_5H_4)Zr(S_2CNBz_2)_3, Mr=987.55, space group P1, a=13.002(4), b=13.659(3), c=29.685(8); α=100.72(2)~o,β=97.23(2)~o, γ=105.36(2)~o; V=4909(2)~3, Z=4, Dc=1.34gcm^(-3), Mo-K(λ=0.71073A) radiation, μ=5.0cm^(-1...(CH_3C_5H_4)Zr(S_2CNBz_2)_3, Mr=987.55, space group P1, a=13.002(4), b=13.659(3), c=29.685(8); α=100.72(2)~o,β=97.23(2)~o, γ=105.36(2)~o; V=4909(2)~3, Z=4, Dc=1.34gcm^(-3), Mo-K(λ=0.71073A) radiation, μ=5.0cm^(-1), R=0.069, Rw=0.078 for 6100 reflections. The title complex has pentagonal bipyramid configuration in which the zirconium atom is coordinated by one CH_3C_5H_4 group and three bidentate dibenzyldithiocarbamate ligands.展开更多
Cp;ZrCl（S;CNBz;） is a five-coordinate bent zirconocene in which the dibenzyldithiocarbamate is a bidentate ligand (Zr-Cl 2.549（1）A; Zr-C 2.489-2.533; Zr-S 2.667（1）, 2.734（1）; Zr-Cl-S1 137.6（1）;; Zr-Cl-S2 73....Cp;ZrCl（S;CNBz;） is a five-coordinate bent zirconocene in which the dibenzyldithiocarbamate is a bidentate ligand (Zr-Cl 2.549（1）A; Zr-C 2.489-2.533; Zr-S 2.667（1）, 2.734（1）; Zr-Cl-S1 137.6（1）;; Zr-Cl-S2 73.3（1）;).展开更多
The compound phenol,2-[4（S）-4,5-dihydro-4-phenyl-2-ozazolinyl（1,C15H13NO2） was synthesized with a simple,one step method free of water and air.It was obtained in a moderate yield from the reaction of 2-hydroxybenz...The compound phenol,2-[4（S）-4,5-dihydro-4-phenyl-2-ozazolinyl（1,C15H13NO2） was synthesized with a simple,one step method free of water and air.It was obtained in a moderate yield from the reaction of 2-hydroxybenzonitrile with optically active amino alcohol in chloroben-zene under dry,anaerobic conditions.It belongs to the orthorhombic system,space group P212121 with a = 5.786（5）,b = 10.730（5）,c = 19.722（5）,C15H13NO2,Mr = 239.26,V = 1224.4（12）3,Z = 4 and Dc = 1.298 mg/m3.The final R = 0.0324 for 1627 observed reflections with Ⅰ 〉 2σ（Ⅰ） and Rw = 0.0826 for all data.The structure of compound 1 was determined by X-ray diffraction,NMR and HRMS.展开更多
The Sèmè oilfield is located in Benin’s offshore coastal sedimentary basin, near the Benin-Nigeria border, and contains two important oil bearing structures called “Sèmè North” and “Sèm...The Sèmè oilfield is located in Benin’s offshore coastal sedimentary basin, near the Benin-Nigeria border, and contains two important oil bearing structures called “Sèmè North” and “Sèmè South”. In this coastal basin, Turonian sandstones of Abeokuta formation (Cenomanian-Turonian to Early Senonian age) form two reservoir units differentiated by two seismic horizons H6 and H6.5. The H6 seismic horizon represents the upper reservoir unit and is the main reservoir from which, more than 22 million barrels of crude oil had previously been produced in Sèmè oilfield. In order to improve knowledge of field petroleum geology, the present study presents the structural features of this upper reservoir unit. The use of Petrel software modules for the integration of 15 wells data, allowed presenting a structural model and illustrative cross sections that precise the geometry and specifying the structural characteristics of this reservoir unit within Sèmè field. The displayed structural architecture shows that the upper Turonian sandstones unit is composed of 11 layers including 7 reservoir layers (A, B, C1, C2, D1, D2, E) and 4 intra-reservoir layers (1, 2, 3 and 4) controlled by faults systems. The model provides basic framework necessary for geological characterization of the reservoir through a static model. The results of this study can be used for petrophysical modeling, Gross Rock Volume (GRV) determination and technical redevelopment of the field.展开更多
基金Supported by the NNSF of China(10626017)the Science Foundation of the Education Committee of Heilongjiang Province(11511276)the Foundation of Heilongjiang Province(LBH-Q05114).
文摘A new computational algorithm is introduced for solving scattering problem in periodic structure. The PML technique is used to deal with the difficulty on truncating the unbounded domain while the DSC algorithm is utilized for the spatial discretization. The present study reveals that the method is efficient for solving the problem.
基金supported by the National Science Foundation of China under Grant No. U1435206 and No. 51672064the Beijing Municipal Science & Technology Commission under grant number Z151100003315012 and D161100002416001
文摘Layered compounds play pivotal roles as precursors for producing 2D materials through mechanical exfoliation(micro-mechanical cleavage) or chemical approaches. Therefore, searching for layered compounds with sharp anisotropic chemical bonding and properties becomes emergent. In this work, the stability, electronic structure, elastic properties, and lattice dynamics of YBCwere investigated. Strong anisotropy in elastic properties is revealed, i.e., high Young’s modulus in a-b plane but low Young’s modulus in c direction. The maximum to minimum Young’s modulus ratio is 2.41 and 2.45 for YBCwith P42/mmc and P4/mbm symmetry, respectively. The most likely systems for shear sliding or microdelaminating are(001)[100] and(001)[010]. The anisotropic elastic properties are underpinned by the anisotropic chemical bonding, i.e., strong bonding within the BCnets and weak bonding between Y atom layers and BCnets. YBCis electrically conductive and the contributions to the electrical conductivity are from delocalized Y 4deas well as Bpandpzelectrons. The layered crystal structure, sharp anisotropic mechanical properties, and metallic conductivity endorse YBCpromising as a precursor for new 2D BCnets.
基金Funded by the National Basic Research Program of China (973 Program) (No. 2009CB623201)the National Natural Science Foundation of China (No.51072150)
文摘The samples of the C-S-H series were synthesized by hydrothermal reaction of fumed silica, CaO and deionized water at initial C/S ratios between 1.0-1.7. Phase composition and structural and morphology characteristics of C-S-H samples were analyzed by XRD, IR and SEM. The experimental results showed that the d-spacing of （002）, （110） and （020） decreased, the d-spacing of （200） increased, and the d-spacing of （310） varied randomly, the polymerization of silica tetrahedra of C-S-H decreased, and morphology of C-S-H samples varied from sheet shapes to long reticular fibers as C/S ratio increased.
基金funded by the Norwegian University of Life Sciences(NMBU)a strategic institutional research program at the Norwegian Institute of Bioeconomy Research(NIBIO).
文摘A key property of the boreal forest is that it stores huge amounts of carbon(C),especially belowground in the soil.Amounts of C stored in the uppermost organic layer of boreal forest soils vary greatly in space due to an interplay between several variables facilitating or preventing C accumulation.In this study,we split C stocks into the organic layer and charcoal C due to their difference in origin,stability,and ecological properties.We compared organic layer C and charcoal C stocks in two regions of south-central Norway(Trillemarka and Varaldskogen),characterized by Scots pine and Norway spruce forests with varying fire histories.We used structural equation modeling to investigate how vegetation composition,hydrotopography,and soil properties interplay to shape organic layer C and charcoal C stocks.Pine forests consistently contained larger organic layer C stocks than spruce forests.Charcoal stocks,in contrast,were less consistent across both forest types and study regions as pine forests had higher charcoal C stocks than spruce forests in Trillemarka,while the two forest types contained equal charcoal C stocks in Varaldskogen.Charcoal and soil organic layer C stocks increased with higher fire frequencies(number of fire events over the last 600 years),but not with a shorter time since last fire(TSF).Additionally,vegetation composition,terrain slope,and soil moisture were the most important drivers of the organic layer C stocks,while charcoal C stocks were mainly controlled by the depth of the organic layer.Also,microtopography was of importance for organic layer C and charcoal C,since depressions in the forest floor had more charcoal C than well-drained minor hills.
文摘According to specifications for Welding Procedure Qualification of ASME IX Section and Chinese code, JB 4708 2000, a software package for managing welding documents has been rebuilt. Consequently, the new software package can be used in a Limited Area Network (LAN) with 4 different levels of authorities for different users. Therefore, the welding documents, including DWPS (Design for Welding Procedure Specifications), PQRs (Procedure Qualification Records) and WPS (Welding Procedure Specifications) can be shared within a company. At the same time, the system provides users various functions such as browsing, copying, editing, searching and printing records, and helps users to make decision of whether a new PQR test is necessary or not according to the codes above as well. Furthermore, super users can also browse the history of record modification and retrieve the records when needed.
基金State Key Basic Development and Programming Project Mechanism and Prediction of Continental Strong Earthquakes (G1998040705).
文摘Based on S wave records of deep teleseisms on Digital Seismic Network of Shanxi Province, shear wave velocity structures beneath 6 stations were obtained by means of S wave waveform fitting. The result shows that the crust is thick in the studied region, reaching 40 km in thickness under 4 stations. The crust all alternatives high velocity layer with low velocity one. There appear varied velocity structures for different stations, and the stations around the same tectonic region exhibit similar structure characteristics. Combined with dominant depth distribution of many small-moderate earthquakes, the correlation between seismogenic layers and crustal structures of high and low velocity layers has been discussed.
基金This project was supported by the China Postdoctoral Science Foundation,Henan Postdoctoral Science Foundation,NCWU 2017 Annual Teaching Teacher Training Object ProjectKey Research Projects of Higher Education in Henan Province(18B150010)+1 种基金the Key Scientific Research Project of Henan Higher Education(No.17A520011)the Science and Technology Research Project of Henan Province(182102110029)
文摘Impurity formation energy, electronic structure, and photocatalytic properties of C-, N-, or S-doped BiOCl are investigated by density-functional theory plus U calculations(DFT + U). Results show that the doping effect of S is better than that of C or N on the tunable photocatalytic activities of BiOCl. At low concentration, S-doped BiOCl systems are the most stable under Bi-rich growth conditions because of their lower impurity-formation energy. Compared with the electronic structures of S-doped BiOCl, C-or N-doped BiOCl have relatively deeper impurity energy levels appearing in their band gap(except Bi_(36)O_(35)NCl_(36)), which may act as photogenerated carrier-recombination centers and reduce photocatalytic activity. At high concentration, S is substituted on the O lattice site system, whereas some S 3p states mix with the valence band; this mixture leads to an obvious band-gap decrease and continuum-state formation above the valence-band edge of BiOCl. Such activity is advantageous to photochemical catalysis response. Compared with pure Bi OCl and a low-concentration S-doped system, a high-concentration S-doped system shows an obvious redshift on the absorption edge and has better photocatalytic O_2 evolution performance.
基金Funded by National Natural Science Foundation of China(Nos51072150,51272193)Program for New Century Excellent Talents inUniversity(No.NCET-10-0660)the Fundamental Research Fundsfor the Central Universities(Nos.2012-Ia-010,2013-Ia-015)
文摘The effects of polyaerylamide （PAM） and polyvinyl alcohol （PVA） on morphology and structure of calcium silica~ hydrate with C/S 1.0-1.7 prepared via precipitation in solution were investigated by XRD, FT-IR and TEM techniques. The results show that incorporation of the polymers decreased the order degree, increased the interlayer spacing and disturbed the layered stacking of C-S-H. Interlayer spacing expansion depended on C/S ratios and type of polymer. Interlayer spacing expansion had a minimum at C/S 1.0 and a maximum at C/S 1.3 and 1.5. Interlayer spacing expansion of PAM was bigger than that of PVA with the same C/S. C-S-H added with PVA mainly exhibited foil-like and fibrillar morphology. The fibrils were of variable length from a few tens of nanometers to a few hundreds of nanometers. Fibrils or foils seemed to be longer in the presence of PVA.
文摘(PPh_3)_2Ni(i-mnt),(i-mnt=S_2C=C(CN)_2),Mr=613.43,monoclinic,Pn,a=9.167(3),b=10.872(3), c=18.209(7) ,β=101.46(3)°,V=1779(1) ,Z=2,Dc=1.15 g/cm^3,λ(Moka)=0.71069 ,μ=7.67 cm^(-1), F(000)=648,T=296K,final R=0.060,Rw=0.073 for 1909 observed reflections with Ⅰ≥3σ(Ⅰ).The complex adopts a square planar geometry as its coordination unit,the mean Ni-S and Ni-P distances are 2.216 and 2.221 ,respectivety.
文摘In the paper, dicalcium silicate (C2S) was modified to obtain higher performance, and the solutionizing pattern of BaSO4 in cement clinker was analyzed theoretically. According to experimental results, solutionizing of BaSO4in cement clinker improved crystal plane distance of C2S as well as the relations of coordination. The performance tests show that the strength of C2S modified by BaSO4 changes and the reactivity of C2S increases significantly.
文摘(CH_3C_5H_4)Zr(S_2CNBz_2)_3, Mr=987.55, space group P1, a=13.002(4), b=13.659(3), c=29.685(8); α=100.72(2)~o,β=97.23(2)~o, γ=105.36(2)~o; V=4909(2)~3, Z=4, Dc=1.34gcm^(-3), Mo-K(λ=0.71073A) radiation, μ=5.0cm^(-1), R=0.069, Rw=0.078 for 6100 reflections. The title complex has pentagonal bipyramid configuration in which the zirconium atom is coordinated by one CH_3C_5H_4 group and three bidentate dibenzyldithiocarbamate ligands.
文摘Cp;ZrCl（S;CNBz;） is a five-coordinate bent zirconocene in which the dibenzyldithiocarbamate is a bidentate ligand (Zr-Cl 2.549（1）A; Zr-C 2.489-2.533; Zr-S 2.667（1）, 2.734（1）; Zr-Cl-S1 137.6（1）;; Zr-Cl-S2 73.3（1）;).
文摘The compound phenol,2-[4（S）-4,5-dihydro-4-phenyl-2-ozazolinyl（1,C15H13NO2） was synthesized with a simple,one step method free of water and air.It was obtained in a moderate yield from the reaction of 2-hydroxybenzonitrile with optically active amino alcohol in chloroben-zene under dry,anaerobic conditions.It belongs to the orthorhombic system,space group P212121 with a = 5.786（5）,b = 10.730（5）,c = 19.722（5）,C15H13NO2,Mr = 239.26,V = 1224.4（12）3,Z = 4 and Dc = 1.298 mg/m3.The final R = 0.0324 for 1627 observed reflections with Ⅰ 〉 2σ（Ⅰ） and Rw = 0.0826 for all data.The structure of compound 1 was determined by X-ray diffraction,NMR and HRMS.
文摘The Sèmè oilfield is located in Benin’s offshore coastal sedimentary basin, near the Benin-Nigeria border, and contains two important oil bearing structures called “Sèmè North” and “Sèmè South”. In this coastal basin, Turonian sandstones of Abeokuta formation (Cenomanian-Turonian to Early Senonian age) form two reservoir units differentiated by two seismic horizons H6 and H6.5. The H6 seismic horizon represents the upper reservoir unit and is the main reservoir from which, more than 22 million barrels of crude oil had previously been produced in Sèmè oilfield. In order to improve knowledge of field petroleum geology, the present study presents the structural features of this upper reservoir unit. The use of Petrel software modules for the integration of 15 wells data, allowed presenting a structural model and illustrative cross sections that precise the geometry and specifying the structural characteristics of this reservoir unit within Sèmè field. The displayed structural architecture shows that the upper Turonian sandstones unit is composed of 11 layers including 7 reservoir layers (A, B, C1, C2, D1, D2, E) and 4 intra-reservoir layers (1, 2, 3 and 4) controlled by faults systems. The model provides basic framework necessary for geological characterization of the reservoir through a static model. The results of this study can be used for petrophysical modeling, Gross Rock Volume (GRV) determination and technical redevelopment of the field.
